EP3453680A1 - Ferrite powder, resin composition, electromagnetic shielding material, electronic circuit substrate, electronic circuit component, and electronic device housing - Google Patents
Ferrite powder, resin composition, electromagnetic shielding material, electronic circuit substrate, electronic circuit component, and electronic device housing Download PDFInfo
- Publication number
- EP3453680A1 EP3453680A1 EP17792658.1A EP17792658A EP3453680A1 EP 3453680 A1 EP3453680 A1 EP 3453680A1 EP 17792658 A EP17792658 A EP 17792658A EP 3453680 A1 EP3453680 A1 EP 3453680A1
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- EP
- European Patent Office
- Prior art keywords
- ferrite
- particles
- powdered
- platy
- electromagnetic shielding
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 229910000859 α-Fe Inorganic materials 0.000 title claims abstract description 271
- 239000000463 material Substances 0.000 title claims description 39
- 239000011342 resin composition Substances 0.000 title claims description 27
- 239000000843 powder Substances 0.000 title description 14
- 239000000758 substrate Substances 0.000 title 1
- 239000002245 particle Substances 0.000 claims abstract description 185
- 241000276425 Xiphophorus maculatus Species 0.000 claims abstract description 72
- 229920005989 resin Polymers 0.000 claims abstract description 39
- 239000011347 resin Substances 0.000 claims abstract description 39
- 239000013078 crystal Substances 0.000 claims abstract description 18
- 229910052596 spinel Inorganic materials 0.000 claims abstract description 6
- 239000011029 spinel Substances 0.000 claims abstract description 6
- 239000000945 filler Substances 0.000 claims description 11
- 229910018605 Ni—Zn Inorganic materials 0.000 claims description 4
- 229910007565 Zn—Cu Inorganic materials 0.000 claims description 4
- 230000000694 effects Effects 0.000 claims description 4
- 238000005245 sintering Methods 0.000 description 49
- 238000003801 milling Methods 0.000 description 37
- 239000011230 binding agent Substances 0.000 description 21
- 238000000034 method Methods 0.000 description 21
- 238000004519 manufacturing process Methods 0.000 description 16
- 239000000203 mixture Substances 0.000 description 15
- 230000035699 permeability Effects 0.000 description 15
- 238000001878 scanning electron micrograph Methods 0.000 description 14
- 239000011248 coating agent Substances 0.000 description 13
- 238000000576 coating method Methods 0.000 description 13
- 239000002243 precursor Substances 0.000 description 13
- 239000002994 raw material Substances 0.000 description 13
- 238000010438 heat treatment Methods 0.000 description 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 10
- 239000001301 oxygen Substances 0.000 description 10
- 229910052760 oxygen Inorganic materials 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 8
- 238000005259 measurement Methods 0.000 description 8
- 229920002451 polyvinyl alcohol Polymers 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- 229910000480 nickel oxide Inorganic materials 0.000 description 7
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 6
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 6
- 230000002159 abnormal effect Effects 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000011358 absorbing material Substances 0.000 description 4
- 238000005266 casting Methods 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 238000010304 firing Methods 0.000 description 4
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 4
- 238000010298 pulverizing process Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- -1 fluororesins Polymers 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000001354 calcination Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
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- 238000011156 evaluation Methods 0.000 description 2
- 230000005415 magnetization Effects 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
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- 238000003756 stirring Methods 0.000 description 2
- 229920002799 BoPET Polymers 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
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- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
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- 229910052802 copper Inorganic materials 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
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- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
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- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
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- 239000011159 matrix material Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000008054 signal transmission Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
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- 238000010301 surface-oxidation reaction Methods 0.000 description 1
- 238000010408 sweeping Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 229910003145 α-Fe2O3 Inorganic materials 0.000 description 1
Images
Classifications
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- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K9/00—Screening of apparatus or components against electric or magnetic fields
- H05K9/0073—Shielding materials
- H05K9/0081—Electromagnetic shielding materials, e.g. EMI, RFI shielding
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- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G49/00—Compounds of iron
- C01G49/0018—Mixed oxides or hydroxides
- C01G49/0063—Mixed oxides or hydroxides containing zinc
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- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/12—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
- H01F1/34—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials non-metallic substances, e.g. ferrites
- H01F1/342—Oxides
- H01F1/344—Ferrites, e.g. having a cubic spinel structure (X2+O)(Y23+O3), e.g. magnetite Fe3O4
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- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/12—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
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- H01F1/36—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials non-metallic substances, e.g. ferrites in the form of particles
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- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/12—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
- H01F1/34—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials non-metallic substances, e.g. ferrites
- H01F1/36—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials non-metallic substances, e.g. ferrites in the form of particles
- H01F1/37—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials non-metallic substances, e.g. ferrites in the form of particles in a bonding agent
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- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/12—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
- H01F1/34—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials non-metallic substances, e.g. ferrites
- H01F1/36—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials non-metallic substances, e.g. ferrites in the form of particles
- H01F1/37—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials non-metallic substances, e.g. ferrites in the form of particles in a bonding agent
- H01F1/375—Flexible bodies
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/0213—Electrical arrangements not otherwise provided for
- H05K1/0216—Reduction of cross-talk, noise or electromagnetic interference
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K9/00—Screening of apparatus or components against electric or magnetic fields
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- C01P2002/00—Crystal-structural characteristics
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- C01P2002/32—Three-dimensional structures spinel-type (AB2O4)
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- C01P2004/00—Particle morphology
- C01P2004/01—Particle morphology depicted by an image
- C01P2004/03—Particle morphology depicted by an image obtained by SEM
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- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
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Definitions
- the present invention relates to powdered ferrite, resin compositions, electromagnetic shielding materials, electronic circuit boards, electronic circuit components, and housings for electronic devices comprising the powdered ferrite.
- Ferrite materials have high magnetic permeability, and have been used as electromagnetic wave absorbing materials or electromagnetic shielding materials. It is known about the electromagnetic wave absorbing characteristics of ferrite that the electromagnetic wave absorbing region ranges over a region higher than the natural resonant frequency. It is also known that the shape of ferrite significantly affects the electromagnetic wave absorbing characteristics, and that the orientation of platy or flat ferrite particles prevents leakage of electromagnetic waves because voids between these particles are reduced in size through the orientation. A variety of methods of producing such platy or flat ferrite particles have been proposed.
- Patent Literature 1 JPH10-233309A discloses a flat ferrite powder prepared through milling of a soft magnetic ferrite prepared by casting, wherein the powder has a longitudinal length of 1 to 100 ⁇ m and an aspect ratio of 5 to 100.
- Patent Literature 1 also discloses a method of producing the flat ferrite powder, comprising a melting step of melting a raw material of soft magnetic ferrite under a predetermined atmosphere; a casting step of casting the molten metal prepared in the melting step into a mold pre-heated under a predetermined atmosphere, and cooling the mold under a specific condition to yield an ingot of soft magnetic ferrite; and a pulverizing step of pulverizing the ingot prepared in the casting step with a pulverizer.
- this flat ferrite powder has a high magnetic permeability and flat shape, and therefore, can be contained in a magnetic shielding sheet in an oriented form along the sheet face, improving the magnetic shielding characteristics of the sheet in a frequency range higher than 1000 MHz.
- This method can facilitate the production of the flat ferrite powder only through milling of the ferrite ingot cast under established conditions, without performing hard work, such as milling of spherical powder.
- This method contributes to a simplified process of producing ferrite powder for a magnetic shielding material in the form of a sheet, and thus has high industrial significance.
- Patent Literature 2 JP2001-284118A discloses a powdered ferrite comprising flat ferrite particles, wherein at least part of the flat ferrite particles has the major diameter d in the range of 1 ⁇ m or more and 100 ⁇ m or less, and has a ratio (d/t) of the major diameter d to the thickness t in the range of 2.5 ⁇ (d/t).
- Patent Literature 2 also discloses a method comprising forming a ferrite raw material in a sheet, firing the sheet to form ferrites, and pulverizing the ferrite sheet into ferrite particles containing flat ferrite particles. This method can provide a powdered ferrite suitable for a magnetic composite body having high magnetic permeability or high noise absorbing characteristics in a high frequency bandwidth and further having high reliability in insulation. In addition, the method can provide the powdered ferrite readily and safely.
- Patent Literature 3 JP2000-252113A discloses a powdered soft magnetic ferrite and a composite material comprising the powdered soft magnetic ferrite, wherein the soft magnetic ferrite particles have a plate shape, and has a composition represented by Mg a Cu b Zn c Fe d O 4 (where 0.3 ⁇ a ⁇ 0.5, 0 ⁇ b ⁇ 0.2, 0.4 ⁇ c ⁇ 0.6, and 1.8 ⁇ d ⁇ 2.2).
- the composite material prepared by dispersing the powdered soft magnetic ferrite into a matrix has a relative permeability having a high real part in the low frequency bandwidth, and can absorb electromagnetic waves in a wide bandwidth at a high-frequency.
- the composite material has high workability and flexibility.
- the powdered soft magnetic ferrite is prepared through firing of a ferrite raw material at a temperature of 1200°C or less using platy ⁇ -Fe 2 O 3 as a source of Fe element.
- Patent Literature 4 JP2001-15312A discloses a method of producing a magnetic paste for electromagnetic wave absorption, involving applying a mixed solution of nanoparticulate ferrite and a binder onto a film to form a ferrite sheet; removing the ferrite sheet from the film; pulverizing and subsequently firing the ferrite sheet into ferrite powder; and mixing the ferrite powder with a paste material.
- This method can produce a magnetic paste for electromagnetic wave absorption comprising ferrite particles having an aspect ratio of 10 or more.
- Such a magnetic paste enables absorption of electromagnetic waves at high absorptivity over a wide bandwidth at a high-frequency.
- Patent Literature 5 JP2015-196607A discloses a method of producing a granulated product for platy particles, involving applying a hydrophilic ink containing a filler onto a hydrophobic base, and solidifying the ink into a coating; immersing the coating containing water into a solvent with the base; and recovering the coating. This method is suitable for production of platy ferrite particles used in the applications to electromagnetic wave absorbing materials and electromagnetic shielding materials.
- Patent Literatures listed above disclose platy ferrite particles and methods of producing the particles.
- these ferrite particles cannot be sufficiently dispersed under high content with high orientation of the ferrite particles.
- a higher content of ferrite particles in the resin is desirable to enhance the electromagnetic shielding characteristics.
- the resin cannot be sufficiently spread into voids between the platy particles, precluding high orientation and sufficient dispersion of the ferrite particles. For this reason, platy ferrite particles having electromagnetic shielding characteristics while allowing the resin to spread sufficiently into the voids between the platy particles at a higher filler content are not yet in practical use.
- a powdered ferrite comprising platy ferrite particles having a protrusion having a specific shape on their surfaces in a specific proportion.
- the present inventor also has found that the powdered ferrite has high electromagnetic shielding characteristics, and has completed the present invention.
- an object of the present invention is to provide a powdered ferrite having high dispersibility in a resin and high electromagnetic shielding characteristics.
- Another object of the present invention is to provide a resin composition, an electromagnetic shielding material, an electronic circuit board, an electronic circuit component, and a housing for electronic devices which comprise such a powdered ferrite.
- One aspect according to the present invention is a powdered ferrite comprising platy ferrite particles having a spinel crystal structure, wherein the powdered ferrite comprises at least 50 number % platy ferrite particles each having at least one protrusion on a surface of the particle, and the at least one protrusion has a shape selected from the group consisting of a rectangular pyramid, a truncated rectangular pyramid, an elongated rectangular pyramid, and combinations thereof.
- the powdered ferrite comprises such platy ferrite particles having a protrusion having a specific shape on their surfaces, the powdered ferrite has not only high dispersibility in a resin but also high productivity and high electromagnetic shielding characteristics.
- Another aspect according to the present invention provides a resin composition comprising the powdered ferrite and a resin.
- Still another aspect according to the present invention provides an electromagnetic shielding material comprising the powdered ferrite as a filler.
- a further aspect according to the present invention provides an electronic circuit board, an electronic circuit component, or a housing for electronic devices comprising the powdered ferrite and/or the resin composition and/or the electromagnetic shielding material, wherein the electronic circuit board, electronic circuit component, or housing for electronic devices has an electromagnetic shielding effect.
- Such a resin composition, electromagnetic shielding material, electronic circuit board, electronic circuit component, and housing for electronic devices have flexibility, and can be shaped to have a curved surface. Moreover, the resin composition, electromagnetic shielding material, electronic circuit board, electronic circuit component, and housing for electronic devices can be safely used for a long time without surface oxidation because ferrite, which is an oxide, is used.
- the powdered ferrite according to the present invention comprises platy ferrite particles having a spinel crystal structure, and can be used as a filler for an electromagnetic shielding material.
- This powdered ferrite has high magnetic permeability and high electromagnetic shielding characteristics because ferrite particles contained in the powdered ferrite has a spinel crystal structure. Voids between such ferrite particles having a platy shape are reduced through the orientation of the particles, preventing the leakage of electromagnetic waves.
- the powdered ferrite indicates a mass of ferrite particles, and the ferrite particles indicate individual particles.
- the powdered ferrite contains platy ferrite particles each having at least one protrusion on a surface of the particle. If particles in the powdered ferrite have no protrusion on their surface, then resin cannot sufficiently fill voids between the particles when the powdered ferrite is dispersed in the resin at a high filler content, which results in uneven strength of the resin composition. If such a resin composition is formed to have a curved surface with a desired curvature, the curved surface will be bent in the middle. In addition, the filler localized in the curved surface may cause uneven electromagnetic shielding characteristics. Accordingly, the platy ferrite particles have at least one protrusion on their surfaces.
- any number of protrusions can be present on the surfaces of the particles as long as electromagnetic wave shielding characteristics are satisfied. Typically, 30 protrusions at most are contained.
- the protrusions are formed utilizing abnormal growth during the crystal growth of ferrite. Therefore, the number of protrusions can be controlled through the control of oxygen content during the sintering and/or heat treatment steps in the production of ferrite.
- the powdered ferrite contains platy ferrite particles having protrusions (particles with protrusions) at 50 number % or higher.
- a content of less than 50 number % is more likely to cause the contact of the platy ferrite particles with each other, preventing the resin from filling voids between the particles when the particles are dispersed in a resin.
- the upper limit of the content is not limited. The maximum content may be 100 number %.
- the protrusion has a shape selected from the group consisting of a rectangular pyramid, a truncated rectangular pyramid, an elongated rectangular pyramid, and combinations thereof. These shapes reflect the crystal structure.
- Other rounded protrusions are attributed to grains which are formed through normal crystal growth and are present in the ferrite particles. These rounded protrusions are distinguished from those reflecting the crystal structure described above.
- the protrusion preferably has a height smaller than the thickness of the platy ferrite particle.
- a protrusion reduces the gap distance between the particles when the platy powdered ferrite is dispersed, oriented, and molded in a resin. For this reason, a sufficient amount of filler can be used, and a molded article having a desired thickness can be readily produced.
- the height of the protrusion can be controlled by the temperature during the sintering and/or heat treatment steps in the production of ferrite. A higher treatment temperature can readily produce higher protrusions.
- the height of the protrusion can be measured as follows: A cross-section of a sample is prepared, and the height of the protrusion from the surface of each particle is measured, as in the measurement of the average thickness which will be described later.
- the SEM image may be photographed by the same method as in the measurement of the average thickness described later. If the number of protrusions is small, this may obstruct the observation of a sufficient number of samples in the cross-sectional area. In such a case, an SEM image of particles may be photographed and printed out as in the measurement of the average plate diameter which will be described later.
- the particles substantially standing upright may be selected from the particles in the photographed image, and the thicknesses of the platy particles and the heights of the protrusions may be directly measured with a scale. In either case, 100 particles having protrusions are selected, and the heights of the protrusions of the particles are measured. The arithmetic average of the measured heights is defined as the height of the protrusions.
- the platy ferrite particles have an average particle diameter of preferably 10 to 2000 ⁇ m, more preferably 20 to 1000 ⁇ m, still more preferably 20 to 500 ⁇ m.
- the average particle diameter indicates the average of the lengths of the platy ferrite particles in the major axis direction (average length in the major axis direction).
- An average particle diameter of 10 ⁇ m or more can achieve ferrite particles having a sufficient aspect ratio, which reduce the influence of the demagnetizing field generated by the ferrite particles, and further enhance the electromagnetic shielding characteristics.
- An average particle diameter of 2000 ⁇ m or less can prevent the fusion of the particles during the sintering step in the production of the powdered ferrite, and can reduce the thickness of the particle in the minor axis direction, facilitating the production of the platy particles having a desired thickness.
- the average plate diameter (average length in the major axis direction) can be determined as follows. An SEM image of ferrite particles is photographed with a field emission scanning electron microscope (FE-SEM), and the length is measured for each particle using the automatic particle analyzing function of an energy dispersive X-ray spectrometer (EDX). Among the measured particles excluding those observed in the thickness direction, those fixed in a standing state during the FE-SEM observation, and those including a plurality of particles recognized as one particle, the average of the diameters of 100 platy particles is defined as the average plate diameter.
- FE-SEM field emission scanning electron microscope
- EDX energy dispersive X-ray spectrometer
- the SEM image may be photographed with an FE-SEM SU-8020 made by Hitachi High-Technologies Corporation at an accelerating voltage of 15 KV and a magnification of 200x, and may be subjected to automatic particle analysis over several fields with an EDX X-MAX made by HORIBA, Ltd. while image information is being received from the FE-SEM.
- the platy ferrite particles have an average thickness of preferably 0.5 to 100 ⁇ m, more preferably 1 to 50 ⁇ m, still more preferably 2 to 30 ⁇ m.
- the average thickness indicates the average of the lengths (thicknesses) of the platy ferrite particles in the minor axis direction (average length in the minor axis direction).
- Ferrite particles having an average thickness of 0.5 ⁇ m or higher can further enhance the electromagnetic shielding characteristics of the powdered ferrite. This is because such ferrite particles have sufficient strength to prevent crack during the production of articles.
- ferrite particles having an average thickness of 100 ⁇ m or less can achieve production of molded articles having a smoother curved surface from a resin composition comprising the powdered ferrite containing such ferrite particles. This is because the ferrite particles are less protruding from the curved surface.
- the average thickness (average length in the minor axis direction) of the ferrite particles can be determined as follows. Powdered ferrite (9 g) and powdered resin (1 g) are placed into a 50-cc glass bottle, and are mixed in a ball mill for 30 minutes. The mixture is placed in a die having a diameter of 13 mm, and is molded under a pressure of 30 MPa. The molded article in a vertically standing state is then embedded in a resin such that the cross-section of the molded article can be observed. The molded article is polished with an abrasive machine, and is used as a sample for measuring the thickness of the ferrite particle.
- the sample for measuring the thickness of the ferrite particle is photographed at a magnification of 50x to 800x with an SEM, and the thickness (length in the minor axis direction) of each particle is measured in disregard of protrusions from the particle in the SEM photograph.
- the arithmetic average of the thicknesses of 100 particles is calculated, and is defined as the average thickness of the ferrite particles.
- the magnification of the SEM photograph to be taken can be selected according to the plate diameter and thickness of the particle.
- the platy ferrite particles have an aspect ratio of preferably 4 to 1000, more preferably 4 to 300, still more preferably 5 to 200.
- An aspect ratio of 4 or more can reduce the influence of the demagnetizing field generated by the ferrite particles, and can further enhance the electromagnetic wave shielding characteristics.
- an aspect ratio of 1000 or less can achieve the compatibility between the electromagnetic shielding characteristics and the flexibility of the resin molded article (resin composition).
- the aspect ratio is calculated as a ratio of the average plate diameter to the average thickness (average plate diameter/average thickness) of the platy ferrite particles.
- the platy ferrite particles preferably have indefinite shapes.
- the term "indefinite shape” used herein indicates that the particle has a substantially constant shape in one direction (thickness direction or minor axis direction) and do not have any regular shape, such as a circular or polygonal shape, in the other two directions, in the three-dimensional shape. In this case, the particle has a perimeter consisting of a combination of straight lines and curved lines. When oriented in a specific direction, platy ferrite particles having such an indefinite shape preclude the formation of the voids therebetween, facilitating an enhancement in electromagnetic shielding characteristics.
- the platy ferrite particles have a shape factor SF-2 of preferably 135 to 300, more preferably 140 to 300, still more preferably 140 to 280.
- the shape factor SF-2 is an index indicating the indefinite shape.
- a shape factor SF-2 closer to 100 indicates that the particle has a shape closer to a sphere or a circle.
- a large shape factor SF-2 indicates that the perimeter of the particle has a large deviation from the envelope and increased recessed portions.
- a shape factor SF-2 of 135 or more can produce powdered ferrite at reduced cost, and can further enhance the electromagnetic shielding characteristics.
- ferrite particles having a shape close to a sphere have low productivity, and easily make voids between the ferrite particles through which electromagnetic waves readily pass when the ferrite particles are accumulated to form the electromagnetic shielding material.
- a shape factor SF-2 of 300 or less can further enhance the electromagnetic shielding characteristics. This is because platy ferrite particles tightly packed on a plane prevent an increase in excessively recessed portions, and thus the formation of voids.
- the shape factor SF-2 can be measured as in the measurement of the average plate diameter.
- An SEM image of ferrite particles is photographed with an FE-SEM, and the perimeter and projected area of each particle is measured using the automatic particle analyzing function of an EDX to calculate the shape factor SF-2 of the particle.
- the average of 100 particles is defined as a shape factor SF-2.
- the platy ferrite particles preferably comprise Ni-Zn ferrite or Ni-Zn-Cu ferrite. These ferrites readily cause abnormal crystal growth, and can facilitate the production of a powdered ferrite containing platy ferrite particles having protrusions. Ni-Zn ferrite and Ni-Zn-Cu ferrite more readily cause abnormal crystal growth through control of only the oxygen content, specifically, a reduction of the oxygen content during the sintering step and/or heat treatment steps in the production of ferrite particles. Thus, these ferrites can more readily and effectively form platy ferrite particles having protrusions, compared to Mn-Zn ferrite or Mn ferrite. Ni-Zn ferrite or Ni-Zn-Cu ferrite can have any composition. In a preferred composition, the contents of Fe, Ni, Zn, and Cu elements are 45 to 52 wt%, 5 to 25 wt%, 0.5 to 25 wt%, and 0 to 6 wt%, respectively.
- Resin composition (electromagnetic shielding material)
- the resin composition (resin molded article) according to the present invention is prepared through curing or thermosetting of a composition comprising a mixture of the powdered ferrite and a resin.
- the resin composition desirably contains 50 to 99.5 wt% powdered ferrite. At a content of 50 wt% or more, the composition can sufficiently demonstrate the characteristics of the ferrite. In contrast, a content of 99.5 wt% or less can facilitate the molding of the resin composition.
- the resin used in the resin composition preferably has flexibility. Such a flexible resin enables the resin composition to be processed to have a curved surface.
- Fig. 1 illustrates an example cross-section of the resin composition.
- a resin composition 1a illustrated in Fig. 1 comprises powdered ferrite 2a and resin 3. As described above, the composition 1a of flexible resin can be processed to have a curved surface.
- the resin composition comprising the powdered ferrite as a filler can be used as an electromagnetic shielding material.
- This electromagnetic shielding material can be bonded to base bodies, and has high electromagnetic shielding characteristics derived from the powdered ferrite.
- the electromagnetic shielding material can have high flexibility attributed to high dispersibility of the powdered ferrite. Such high flexibility allows a high degree of freedom in shape of the body to be bonded to, and therefore, the electromagnetic shielding material can be bonded to a base body having a curved surface.
- the electromagnetic shielding material can be bonded to the base body by any means, for example, hydraulic transfer.
- the electronic circuit board, electronic circuit component, and housing for electronic devices according to the present invention comprise the electromagnetic shielding material, and have a high electromagnetic shielding effect. Due to high flexibility of the electromagnetic shielding material, the electronic circuit board, electronic circuit component, and housing for electronic devices according to the present invention have a high degree of freedom in shape, and can have curved surfaces to be bonded to the electromagnetic shielding material.
- Fig. 2 is a sectional view illustrating an example housing for electronic devices which accommodates an electronic circuit.
- the resin composition 1a is disposed on and along the curved outer peripheral surface of an electromagnetic wave shield 8 made of a metal, and serves as an electromagnetic shielding material.
- ferrite raw materials are weighed, and are mixed with a Henschel mixer or the like.
- the ferrite raw materials include, but should not be limited to, metal oxides, metal carbonates, metal hydroxides, and mixtures thereof.
- the mixture of ferrite raw materials can be pelletized with a roll compactor or the like, and is calcined in a rotary kiln or the like. The calcination is performed at a temperature of 1000°C in ambient atmosphere, for example.
- the calcined product is coarsely and then finely milled.
- the water content is adjusted to yield cakes of calcined product.
- a dispersant is added to the cakes of calcined product, and is dispersed with a disperser to prepare aqueous ink.
- a binder is further added thereto to prepare ink for coating.
- the ink for coating is then applied into a predetermined thickness onto a base material, such as a film, using an applicator, for example.
- a PVA aqueous solution is further applied onto the ink coated surface, and water is removed.
- the ink coated surface is peeled off from the base material to yield a platy granulated product (ferrite precursor) before sintering.
- the binder is removed from the platy granulated product (ferrite precursor) before sintering, followed by sintering the platy granulated product.
- the binder removal is preferably performed at a temperature equal to or lower than the sintering temperature preferably under a condition such that the binder component can be removed.
- the sintering can be performed at a temperature of about 800 to 1300°C in an atmosphere where the oxygen content is 20 vol% or less, preferably 3.5 vol% or less. Such a reduced oxygen content can form protrusions accompanied by the abnormal crystal growth.
- the sintering may be performed in ambient atmosphere.
- the ferrite precursor before the sintering and/or the sintered product after the sintering may be milled to adjust the plate diameter, when necessary.
- Platy ferrite particles having a predetermined shape can be readily produced through the milling.
- the ferrite precursor before the sintering and/or the sintered product after the sintering may be milled, and may be classified through a sieve having a predetermined opening to have a target plate diameter.
- the adjustment of the plate diameter through the milling may be performed after the sintering, or may be performed before the binder removal and/or sintering steps to prevent the fusion between the particles during the sintering step.
- the milling performed before the sintering is referred to as pre-sintering milling
- the milling performed after the sintering is referred to as post-sintering milling for clarity, when necessary.
- a heat treatment may be performed after the milling as necessary.
- the direction of crystal growth of the platy ferrite particles is substantially restricted to the plane direction thereof, and therefore, the platy ferrite particles have a crystal structure which is more readily distorted than bulky ferrite. Furthermore, the crystal structure of the ferrite particles is more likely to be distorted through the milling.
- the distortion of the crystal structure can be reduced through the heat treatment performed after the sintering and milling steps.
- the heat treatment may be performed at a temperature of about 800 to 1300°C in an atmosphere where the oxygen content is 20 vol% or less, preferably 3.5 vol% or less. Such a reduced oxygen content can form protrusions accompanied by the abnormal crystal growth.
- the powdered ferrite prepared through these steps comprises platy ferrite particles having protrusions having a specific shape on the surfaces thereof.
- Such a powdered ferrite has high dispersibility in resins and a significantly increased plate diameter, thus achieving high electromagnetic shielding characteristics.
- the powdered ferrite also has high productivity.
- the resin compositions and the electromagnetic shielding materials comprising the powdered ferrite as a filler have high flexibility attributed to high dispersibility of the powdered ferrite, and can be bonded to base bodies (housings) having curved surfaces.
- Patent Literature 2 does not disclose any information on the shape of the particles of the powdered ferrite other than the long diameter, the plate thickness, and the aspect ratio thereof.
- Patent Literature 3 discloses ferrite particles having indefinite shapes and a platy shape.
- a sufficient aspect ratio cannot be achieved due to a significantly small ferrite particle diameter, or the grain size of the ferrite particles cannot be sufficiently ensured due to a significantly low sintering temperature.
- the powdered ferrite may inevitably have a low magnetic permeability, which is used as a substituting index indicating the electromagnetic wave absorbing characteristics.
- the ferrite sheet In the case where the ferrite sheet is prepared by peeling off from the film to obtain the ferrite sheet solely as disclosed in Patent Literature 4, the ferrite sheet could be broken. It is difficult to obtain the powdered ferrite in a stable state. In particular, a thinner ferrite sheet is more difficult to peel off from the base material, imposing more difficulties in the actual production process. To avoid the breakage of the ferrite sheet during the peeling-off stage from the film, a large amount of binder components needs to be added to a mixed coating solution. An increase in binder components will increase the viscosity of the coating solution containing the ferrite raw material. The content of the ferrite raw material in the coating solution could be reduced to adjust the viscosity.
- a powdered ferrite was prepared in accordance with the following procedure. Detailed conditions for production are also shown in Table 1.
- Iron oxide, nickel oxide, zinc oxide, and copper oxide as raw materials were weighed such that the amounts of Fe 2 O 3 , NiO, ZnO, and CuO were 51.5 mol, 15 mol, 30 mol, and 8 mol, respectively, and were mixed with a Henschel mixer.
- the mixture was pelletized with a roll compactor, and was calcined with a rotary kiln in ambient atmosphere at a temperature of 950°C. A calcined product was thereby yielded.
- Ink was prepared from the calcined product.
- the calcined product was coarsely milled with a rod mill, and then finely milled with a wet bead mill.
- the water content was adjusted to give a solid content of 65 wt%.
- Cakes of the calcined product were thereby yielded.
- a dispersant was added to the cakes of the calcined product, and was dispersed with a homogenizer to prepare aqueous ink.
- a poly(vinyl alcohol) (PVA) binder was further added to the aqueous ink in an amount of 5 wt% of the water content in the aqueous ink. Ink for coating was thereby prepared.
- a ferrite precursor was prepared with the resulting ink for coating.
- the ink was applied onto a base material.
- the ink was applied onto a commercially available PET film (thickness: 50 ⁇ m), i.e. base material, with an applicator into a film having a thickness after drying (dry thickness) of 10 ⁇ m.
- dry thickness a thickness after drying
- water was removed from the coated surface.
- a PVA aqueous solution 25 wt% aqueous solution
- the coated surface was peeled off from the base material to prepare a green platy granulated product (ferrite precursor) in the form of a sheet.
- the binder was removed from the ferrite precursor in the air at 650°C.
- the ferrite precursor was then sintered at 1200°C for four hours in an atmosphere containing 0 vol% oxygen, yielding a platy sintered product.
- the platy sintered product was milled (post-sintering milling) to yield a powdered ferrite.
- the sintered and milled product was classified with sieves (36 mesh and 80 mesh) in accordance with Japanese Industrial Standards (JIS).
- the powdered ferrite contained platy ferrite particles having an average thickness of 8 ⁇ m and an average plate diameter of 489 ⁇ m.
- a powdered ferrite was prepared as in Example 1 except that the dry thickness during the application of the ink was 3.5 ⁇ m, the binder was removed at a temperature of 1000°C, and sieves (80 mesh and 250 mesh) in accordance with JIS were used in the milling.
- a powdered ferrite was prepared as in Example 2 except that the sintering was performed in ambient atmosphere, and a heat treatment was performed at 1220°C in an atmosphere containing 0 vol% oxygen after the milling.
- a powdered ferrite was prepared as in Example 1 except that raw materials, i.e., iron oxide (Fe 2 O 3 ), nickel oxide (NiO), zinc oxide (ZnO), and copper oxide (CuO) were compounded in amounts of 49 mol, 15 mol, 30 mol, and 6 mol, respectively, the dry thickness after the application of the ink was 9 ⁇ m, and sieves (80 mesh and 250 mesh) in accordance with JIS were used in the milling.
- raw materials i.e., iron oxide (Fe 2 O 3 ), nickel oxide (NiO), zinc oxide (ZnO), and copper oxide (CuO) were compounded in amounts of 49 mol, 15 mol, 30 mol, and 6 mol, respectively, the dry thickness after the application of the ink was 9 ⁇ m, and sieves (80 mesh and 250 mesh) in accordance with JIS were used in the milling.
- a powdered ferrite was prepared as in Example 1 except that raw materials, i.e., iron oxide (Fe 2 O 3 ), nickel oxide (NiO), zinc oxide (ZnO), and copper oxide (CuO) were compounded in amounts of 52.75 mol, 15 mol, 30 mol, and 9 mol, respectively, the dry thickness during the application of the ink was 11 ⁇ m, and sieves in accordance with JIS (250 mesh and 350 mesh) were used in the milling.
- raw materials i.e., iron oxide (Fe 2 O 3 ), nickel oxide (NiO), zinc oxide (ZnO), and copper oxide (CuO) were compounded in amounts of 52.75 mol, 15 mol, 30 mol, and 9 mol, respectively, the dry thickness during the application of the ink was 11 ⁇ m, and sieves in accordance with JIS (250 mesh and 350 mesh) were used in the milling.
- a powdered ferrite was prepared as in Example 2 except that the milling before sintering (pre-sintering milling) was performed rather than the milling after the sintering (post-sintering milling).
- pre-sintering milling a ferrite precursor after the binder removal was milled, and was classified with sieves (36 mesh and 80 mesh) in accordance with JIS.
- a powdered ferrite was prepared as in Example 2 except that the sintering temperature was 1090°C, and sieves (36 mesh and 80 mesh) in accordance with JIS were used in the milling.
- a powdered ferrite was prepared as in Example 7 except that the sintering temperature was 1250°C.
- a powdered ferrite was prepared as in Example 2 except that the sintering was performed in an atmosphere containing 8 vol% oxygen, and the milling (post-sintering milling) was not performed.
- a powdered ferrite was prepared as in Example 1 except that the binder was removed at a temperature of 1000°C and the sintering was performed in ambient atmosphere.
- a powdered ferrite was prepared as in Example 10 except that a heat treatment was performed at 1220°C in ambient atmosphere after the milling (post-sintering milling) was performed.
- a powdered ferrite was prepared as in Example 2 except that the PVA aqueous solution was not applied during the preparation of the ferrite precursor, the sintering was performed in ambient atmosphere, and a sieve (350 mesh) in accordance with JIS was used in the milling (post-sintering milling).
- a powdered ferrite was prepared as in Example 1 except that the binder was removed at a temperature of 1000°C and the sintering temperature was 1050°C.
- a powdered ferrite was prepared as in Example 13 except that the sintering temperature was 1310°C.
- the composition of the powdered ferrite was determined by chemical analysis. Ferrite particles (0.2 g) were weighed, and were completely dissolved in a heated solution of 1N hydrochloric acid (20 ml) and 1N nitric acid (20 ml) in pure water (60 ml) to prepare an aqueous solution. The contents of the metal elements in the aqueous solution were determined with an ICP analyzer (SHIMADZU Corporation, ICPS-1000IV). Similarly, the contents of the metal elements in Examples and Comparative Examples described later were also determined.
- the average plate diameter and the shape factor SF-2 were determined at the same time .
- An SEM image of ferrite particles was photographed with an FE-SEM.
- the length, perimeter, and projected area of each particle were measured using the automatic particle analyzing function of an EDX to calculate the length of each particle.
- the lengths of 100 particles were averaged to determine the average plate diameter.
- the SF-2 was determined from the perimeter and projected area of each particle, and the average of 100 particles was defined as a shape factor SF-2.
- the SEM image was photographed with an FE-SEM SU-8020 made by Hitachi High-Technologies Corporation at an accelerating voltage of 15 KV and a magnification of 200x, and was subjected to particle analysis with an EDX X-MAX made by HORIBA, Ltd. while image information was being received from the FE-SEM.
- the average thickness of the platy ferrite particles was determined as follows. Powdered ferrite (9 g) and powder resin (1 g) were placed into a 50-cc glass bottle, and were mixed in a ball mill for 30 minutes. The mixture was placed into a die having a diameter of 13 mm, and was molded under a pressure of 30 MPa. The molded article in a vertically standing state was then embedded in a resin such that the cross-section of the molded article was observed. The molded article was polished with an abrasive machine, and was used as a sample for measuring the thickness of the ferrite particle.
- the sample for measuring the thickness of the ferrite particle was photographed at a magnification of 50x to 800x with an SEM, and the thickness (length in the minor axis direction) of each particle was measured in disregard of protrusions from the particle in the SEM image.
- the arithmetic average of the thicknesses of 100 particles was calculated, and was defined as the average thickness of the ferrite particles.
- the aspect ratio of the platy ferrite particles was calculated as an aspect ratio (average plate diameter)/(average thickness) from the average plate diameter and the average thickness described above.
- the heights of protrusions of the platy ferrite particles were determined as follows: A cross-section of a sample was prepared as in the determination of the average thickness of the platy ferrite particles, and the heights of the protrusions from the surfaces of the particle were measured. An SEM image was photographed as described above. In the case where the number of protrusions is small, it is difficult to observe a sufficient number of samples in the cross-sectional area. In such a case, an SEM image of particles was photographed as in the determination of the average plate diameter, and was printed out. The particles substantially standing upright were selected from the photographed image, and the thicknesses of the platy particles and the heights of the protrusions were directly measured with a scale. In either case, 100 particles having protrusions were selected, and the heights of the protrusions of the particles were measured. The arithmetic average was defined as the height of the protrusions.
- the proportion of platy ferrite particles (particles with protrusions) each having at least one protrusion on the surface thereof contained in the powdered ferrite was determined as follows: An SEM image was photographed as in the measurement of the height of protrusions. The total number of particles and the number of particles with protrusions in the SEM image were visually counted. The proportion of the particles with protrusions was calculated from (the number of particles with protrusions)/(the total number of particles).
- the magnetic characteristics of the powdered ferrite were measured with a vibrating sample magnetometer (Toei Industry Co., Ltd., VSM-C7-10A).
- a sample (powdered ferrite) was filled in a cell having an inner diameter of 5 mm and a height of 2 mm. The cell was placed in the magnetometer. During the measurement, a magnetic field was applied, and was swept up to 5 K ⁇ 1000/4 ⁇ A/m. In the next step, the applied magnetic field was decreased to print a hysteresis curve on a recording paper. From the data in this curve, the magnetization ( ⁇ s) was read at an applied magnetic field of 5 K ⁇ 1000/4 ⁇ A/m. The residual magnetization ( ⁇ r) and the coercive force (Hc) were also obtained.
- the frequency characteristics of the powdered ferrite were determined through the measurement of the complex magnetic permeability of the powdered ferrite.
- a sample was prepared as follows. Powdered ferrite (9 g) and binder resin (Kynar301F: poly(vinylidene fluoride)) (1 g) were weighed, were placed into a 50-cc glass bottle, and were mixed under stirring with a ball mill at 100 rpm for 30 minutes. After stirring, about 0.6 g of the mixture was weighed, and was placed into a die having an inner diameter of 4.5 mm and an outer diameter of 13 mm. The mixture was pressed with a press under a pressure of 40 MPa for one minute.
- the molded article was settled in a hot air dryer at 140°C for two hours to prepare a sample for measuring the complex magnetic permeability.
- the complex magnetic permeability was measured with an RF impedance/material analyzer (Agilent Technologies, Inc., E4991A) and a measuring electrode for a magnetic material (Agilent Technologies, Inc., 16454A).
- the outer diameter, the length in the minor axis direction, and the inner diameter of the sample were measured, and were input into the analyzer.
- the complex magnetic permeability (real part ⁇ ' and imaginary part ⁇ " of the magnetic permeability) was measured at an amplitude of 100 mV where sweeping was performed in the range of 1 MHz to 1 GHz in logarithmic terms. Table 2 shows the magnetic permeabilities ⁇ ' and ⁇ " at 13.56 MHz.
- the flexibility of the resin molded article comprising the powdered ferrite was evaluated.
- the resin molded article was prepared as follows: A binder resin (10 wt% PVA aqueous solution) (45 g) and powdered ferrite (5 g) were mixed to disperse the powdered ferrite. The dispersion was suction-filtered through a Nutsche funnel having a diameter of 180 mm to deposit a layer of platy ferrite particles containing the binder resin on a filter paper. The layer of the platy ferrite particles was dried to remove water. The layer was then peeled off from the filter paper, and was cut into a 30 mm square to prepare a sheet containing the platy ferrite particles. The sheet was used as a resin molded article. The resin molded article was then bent along an acrylic round bar having a diameter of 20 mm to evaluate the flexibility. The flexibility was ranked according to the following criteria:
- the powdered ferrites in Examples 1 to 9 had not only superior magnetic characteristics and frequency characteristics but also high flexibility in the form of the resin molded articles.
- the powdered ferrites in Examples 10 to 13 had poor flexibility in the form of the resin molded articles, i.e., were cracked or broken.
- powdered ferrite was not yielded because of the fusion between the particles during the sintering step.
- FIG. 3 An SEM image of the powdered ferrite in Example 1 is shown in Fig. 3.
- Fig. 3 demonstrates that individual platy ferrite particles have indefinite shapes, and each have at least one protrusion on its surface, the at least one protrusion having a shape selected from the group consisting of a rectangular pyramid, a truncated rectangular pyramid, an elongated rectangular pyramid, and combinations thereof.
- Example 2 Furthermore, the resin molded article prepared in Example 2 was put on water, and was bonded onto the surface of a plastic base body through hydraulic transfer to prepare a housing. Although the housing had a curved surface, the ferrite particles were successfully bonded to the housing along the curved surface. It was confirmed that the ferrite particles are applicable to curved surfaces without difficulty.
- Table 1 Amounts Calcining Preparation of ink Preparation of ferrite precursor Binder removal Pre-sintering milling Sintering Post-sintering milling Heat treatment Fe 2 O 3 (mol) NiO (mol) ZnO (mol) CuO (mol) Temp. (°C) Atmosphere Particle diameter in Slurry ( ⁇ m) Ink Viscosity (cps) Ink Coating thickness (dry thickness, ⁇ m) PVA Coating thickness (wet thickness, ⁇ m) Temp. (°C) Atmosphere Milliing condition (mesh) Temp. (°C) Atmosphere (O 2 content) Milling condition (mesh) Temp. (°C) Atmosphere (O 2 content) Ex.
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Abstract
Description
- The present invention relates to powdered ferrite, resin compositions, electromagnetic shielding materials, electronic circuit boards, electronic circuit components, and housings for electronic devices comprising the powdered ferrite.
- Accompanied by digitalization, an improvement in performance, and a reduction in size of recent electronic communication devices, there have been concerns about malfunctions of these devices and adverse effects over human bodies which are caused by noises or electromagnetic waves generated from their neighboring devices. Such concerns have led to an increasing demand for electromagnetic wave absorbing materials and electromagnetic shielding materials which prevent leakage of electromagnetic waves from their sources or shield external electromagnetic waves. In particular, an increase in data transfer rate and processing rate leads to high-rate transmission of signals at higher frequencies, and accordingly, electromagnetic wave absorbing materials and electromagnetic shielding materials exhibiting high performance at high-frequency regions have been required.
- Ferrite materials have high magnetic permeability, and have been used as electromagnetic wave absorbing materials or electromagnetic shielding materials. It is known about the electromagnetic wave absorbing characteristics of ferrite that the electromagnetic wave absorbing region ranges over a region higher than the natural resonant frequency. It is also known that the shape of ferrite significantly affects the electromagnetic wave absorbing characteristics, and that the orientation of platy or flat ferrite particles prevents leakage of electromagnetic waves because voids between these particles are reduced in size through the orientation. A variety of methods of producing such platy or flat ferrite particles have been proposed.
- For example, Patent Literature 1 (JPH10-233309A) discloses a flat ferrite powder prepared through milling of a soft magnetic ferrite prepared by casting, wherein the powder has a longitudinal length of 1 to 100 µm and an aspect ratio of 5 to 100. Patent Literature 1 also discloses a method of producing the flat ferrite powder, comprising a melting step of melting a raw material of soft magnetic ferrite under a predetermined atmosphere; a casting step of casting the molten metal prepared in the melting step into a mold pre-heated under a predetermined atmosphere, and cooling the mold under a specific condition to yield an ingot of soft magnetic ferrite; and a pulverizing step of pulverizing the ingot prepared in the casting step with a pulverizer. According to Patent Literature 1, this flat ferrite powder has a high magnetic permeability and flat shape, and therefore, can be contained in a magnetic shielding sheet in an oriented form along the sheet face, improving the magnetic shielding characteristics of the sheet in a frequency range higher than 1000 MHz. This method can facilitate the production of the flat ferrite powder only through milling of the ferrite ingot cast under established conditions, without performing hard work, such as milling of spherical powder. This method contributes to a simplified process of producing ferrite powder for a magnetic shielding material in the form of a sheet, and thus has high industrial significance.
- Patent Literature 2 (
JP2001-284118A - Patent Literature 3 (
JP2000-252113A - Other methods of producing platy ferrite powder are disclosed, which involves applying a ferrite raw material comprising a variety of metal oxides or calcined powder in an organic solvent onto a base, removing the organic solvent, and firing the ferrite raw material. For example, Patent Literature 4 (
JP2001-15312A - Patent Literature 5 (
JP2015-196607A -
- Patent Literature 1: JPH10-233309A
- Patent Literature 2:
JP2001-284118A - Patent Literature 3:
JP2000-252113A - Patent Literature 4:
JP2001-15312A - Patent Literature 5:
JP2015-196607A - As described above, Patent Literatures listed above disclose platy ferrite particles and methods of producing the particles. Unfortunately, in the case where these ferrite particles are dispersed in a resin as a filler to prepare a resin composition, these ferrite particles cannot be sufficiently dispersed under high content with high orientation of the ferrite particles. In use as an electromagnetic shielding material, a higher content of ferrite particles in the resin is desirable to enhance the electromagnetic shielding characteristics. At such a higher content, however, the resin cannot be sufficiently spread into voids between the platy particles, precluding high orientation and sufficient dispersion of the ferrite particles. For this reason, platy ferrite particles having electromagnetic shielding characteristics while allowing the resin to spread sufficiently into the voids between the platy particles at a higher filler content are not yet in practical use.
- As a result of extensive research, the present inventor has found that the above problems are solved by a powdered ferrite comprising platy ferrite particles having a protrusion having a specific shape on their surfaces in a specific proportion. The present inventor also has found that the powdered ferrite has high electromagnetic shielding characteristics, and has completed the present invention.
- Accordingly, an object of the present invention is to provide a powdered ferrite having high dispersibility in a resin and high electromagnetic shielding characteristics. Another object of the present invention is to provide a resin composition, an electromagnetic shielding material, an electronic circuit board, an electronic circuit component, and a housing for electronic devices which comprise such a powdered ferrite.
- One aspect according to the present invention is a powdered ferrite comprising platy ferrite particles having a spinel crystal structure,
wherein the powdered ferrite comprises at least 50 number % platy ferrite particles each having at least one protrusion on a surface of the particle, and the at least one protrusion has a shape selected from the group consisting of a rectangular pyramid, a truncated rectangular pyramid, an elongated rectangular pyramid, and combinations thereof. - Since the powdered ferrite comprises such platy ferrite particles having a protrusion having a specific shape on their surfaces, the powdered ferrite has not only high dispersibility in a resin but also high productivity and high electromagnetic shielding characteristics.
- Another aspect according to the present invention provides a resin composition comprising the powdered ferrite and a resin.
- Still another aspect according to the present invention provides an electromagnetic shielding material comprising the powdered ferrite as a filler.
- A further aspect according to the present invention provides an electronic circuit board, an electronic circuit component, or a housing for electronic devices comprising the powdered ferrite and/or the resin composition and/or the electromagnetic shielding material, wherein the electronic circuit board, electronic circuit component, or housing for electronic devices has an electromagnetic shielding effect.
- Such a resin composition, electromagnetic shielding material, electronic circuit board, electronic circuit component, and housing for electronic devices have flexibility, and can be shaped to have a curved surface. Moreover, the resin composition, electromagnetic shielding material, electronic circuit board, electronic circuit component, and housing for electronic devices can be safely used for a long time without surface oxidation because ferrite, which is an oxide, is used.
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Fig. 1 is a sectional view illustrating a resin composition. -
Fig. 2 is a sectional view illustrating a housing for electronic devices. -
Fig. 3 is an SEM image of powdered ferrite prepared in Example 1. - The powdered ferrite according to the present invention comprises platy ferrite particles having a spinel crystal structure, and can be used as a filler for an electromagnetic shielding material. This powdered ferrite has high magnetic permeability and high electromagnetic shielding characteristics because ferrite particles contained in the powdered ferrite has a spinel crystal structure. Voids between such ferrite particles having a platy shape are reduced through the orientation of the particles, preventing the leakage of electromagnetic waves. Throughout the specification, the powdered ferrite indicates a mass of ferrite particles, and the ferrite particles indicate individual particles.
- The powdered ferrite contains platy ferrite particles each having at least one protrusion on a surface of the particle. If particles in the powdered ferrite have no protrusion on their surface, then resin cannot sufficiently fill voids between the particles when the powdered ferrite is dispersed in the resin at a high filler content, which results in uneven strength of the resin composition. If such a resin composition is formed to have a curved surface with a desired curvature, the curved surface will be bent in the middle. In addition, the filler localized in the curved surface may cause uneven electromagnetic shielding characteristics. Accordingly, the platy ferrite particles have at least one protrusion on their surfaces. As an upper limit, any number of protrusions can be present on the surfaces of the particles as long as electromagnetic wave shielding characteristics are satisfied. Typically, 30 protrusions at most are contained. The protrusions are formed utilizing abnormal growth during the crystal growth of ferrite. Therefore, the number of protrusions can be controlled through the control of oxygen content during the sintering and/or heat treatment steps in the production of ferrite.
- The powdered ferrite contains platy ferrite particles having protrusions (particles with protrusions) at 50 number % or higher. A content of less than 50 number % is more likely to cause the contact of the platy ferrite particles with each other, preventing the resin from filling voids between the particles when the particles are dispersed in a resin. The upper limit of the content is not limited. The maximum content may be 100 number %.
- Since the ferrite particles have a spinel crystal structure, the protrusion has a shape selected from the group consisting of a rectangular pyramid, a truncated rectangular pyramid, an elongated rectangular pyramid, and combinations thereof. These shapes reflect the crystal structure. Other rounded protrusions are attributed to grains which are formed through normal crystal growth and are present in the ferrite particles. These rounded protrusions are distinguished from those reflecting the crystal structure described above.
- In the powdered ferrite according to the present invention, the protrusion preferably has a height smaller than the thickness of the platy ferrite particle. Such a protrusion reduces the gap distance between the particles when the platy powdered ferrite is dispersed, oriented, and molded in a resin. For this reason, a sufficient amount of filler can be used, and a molded article having a desired thickness can be readily produced. The height of the protrusion can be controlled by the temperature during the sintering and/or heat treatment steps in the production of ferrite. A higher treatment temperature can readily produce higher protrusions.
- The height of the protrusion can be measured as follows: A cross-section of a sample is prepared, and the height of the protrusion from the surface of each particle is measured, as in the measurement of the average thickness which will be described later. The SEM image may be photographed by the same method as in the measurement of the average thickness described later. If the number of protrusions is small, this may obstruct the observation of a sufficient number of samples in the cross-sectional area. In such a case, an SEM image of particles may be photographed and printed out as in the measurement of the average plate diameter which will be described later. The particles substantially standing upright may be selected from the particles in the photographed image, and the thicknesses of the platy particles and the heights of the protrusions may be directly measured with a scale. In either case, 100 particles having protrusions are selected, and the heights of the protrusions of the particles are measured. The arithmetic average of the measured heights is defined as the height of the protrusions.
- The platy ferrite particles have an average particle diameter of preferably 10 to 2000 µm, more preferably 20 to 1000 µm, still more preferably 20 to 500 µm. The average particle diameter indicates the average of the lengths of the platy ferrite particles in the major axis direction (average length in the major axis direction). An average particle diameter of 10 µm or more can achieve ferrite particles having a sufficient aspect ratio, which reduce the influence of the demagnetizing field generated by the ferrite particles, and further enhance the electromagnetic shielding characteristics. An average particle diameter of 2000 µm or less can prevent the fusion of the particles during the sintering step in the production of the powdered ferrite, and can reduce the thickness of the particle in the minor axis direction, facilitating the production of the platy particles having a desired thickness.
- The average plate diameter (average length in the major axis direction) can be determined as follows. An SEM image of ferrite particles is photographed with a field emission scanning electron microscope (FE-SEM), and the length is measured for each particle using the automatic particle analyzing function of an energy dispersive X-ray spectrometer (EDX). Among the measured particles excluding those observed in the thickness direction, those fixed in a standing state during the FE-SEM observation, and those including a plurality of particles recognized as one particle, the average of the diameters of 100 platy particles is defined as the average plate diameter. The SEM image may be photographed with an FE-SEM SU-8020 made by Hitachi High-Technologies Corporation at an accelerating voltage of 15 KV and a magnification of 200x, and may be subjected to automatic particle analysis over several fields with an EDX X-MAX made by HORIBA, Ltd. while image information is being received from the FE-SEM.
- The platy ferrite particles have an average thickness of preferably 0.5 to 100 µm, more preferably 1 to 50 µm, still more preferably 2 to 30 µm. The average thickness indicates the average of the lengths (thicknesses) of the platy ferrite particles in the minor axis direction (average length in the minor axis direction). Ferrite particles having an average thickness of 0.5 µm or higher can further enhance the electromagnetic shielding characteristics of the powdered ferrite. This is because such ferrite particles have sufficient strength to prevent crack during the production of articles. In contrast, ferrite particles having an average thickness of 100 µm or less can achieve production of molded articles having a smoother curved surface from a resin composition comprising the powdered ferrite containing such ferrite particles. This is because the ferrite particles are less protruding from the curved surface.
- The average thickness (average length in the minor axis direction) of the ferrite particles can be determined as follows. Powdered ferrite (9 g) and powdered resin (1 g) are placed into a 50-cc glass bottle, and are mixed in a ball mill for 30 minutes. The mixture is placed in a die having a diameter of 13 mm, and is molded under a pressure of 30 MPa. The molded article in a vertically standing state is then embedded in a resin such that the cross-section of the molded article can be observed. The molded article is polished with an abrasive machine, and is used as a sample for measuring the thickness of the ferrite particle. The sample for measuring the thickness of the ferrite particle is photographed at a magnification of 50x to 800x with an SEM, and the thickness (length in the minor axis direction) of each particle is measured in disregard of protrusions from the particle in the SEM photograph. The arithmetic average of the thicknesses of 100 particles is calculated, and is defined as the average thickness of the ferrite particles. The magnification of the SEM photograph to be taken can be selected according to the plate diameter and thickness of the particle.
- The platy ferrite particles have an aspect ratio of preferably 4 to 1000, more preferably 4 to 300, still more preferably 5 to 200. An aspect ratio of 4 or more can reduce the influence of the demagnetizing field generated by the ferrite particles, and can further enhance the electromagnetic wave shielding characteristics. In contrast, an aspect ratio of 1000 or less can achieve the compatibility between the electromagnetic shielding characteristics and the flexibility of the resin molded article (resin composition). The aspect ratio is calculated as a ratio of the average plate diameter to the average thickness (average plate diameter/average thickness) of the platy ferrite particles.
- The platy ferrite particles preferably have indefinite shapes. The term "indefinite shape" used herein indicates that the particle has a substantially constant shape in one direction (thickness direction or minor axis direction) and do not have any regular shape, such as a circular or polygonal shape, in the other two directions, in the three-dimensional shape. In this case, the particle has a perimeter consisting of a combination of straight lines and curved lines. When oriented in a specific direction, platy ferrite particles having such an indefinite shape preclude the formation of the voids therebetween, facilitating an enhancement in electromagnetic shielding characteristics.
- The platy ferrite particles have a shape factor SF-2 of preferably 135 to 300, more preferably 140 to 300, still more preferably 140 to 280. The shape factor SF-2 is an index indicating the indefinite shape. A shape factor SF-2 closer to 100 indicates that the particle has a shape closer to a sphere or a circle. In contrast, a large shape factor SF-2 indicates that the perimeter of the particle has a large deviation from the envelope and increased recessed portions. A shape factor SF-2 of 135 or more can produce powdered ferrite at reduced cost, and can further enhance the electromagnetic shielding characteristics. This is because ferrite particles having a shape close to a sphere have low productivity, and easily make voids between the ferrite particles through which electromagnetic waves readily pass when the ferrite particles are accumulated to form the electromagnetic shielding material. In contrast, a shape factor SF-2 of 300 or less can further enhance the electromagnetic shielding characteristics. This is because platy ferrite particles tightly packed on a plane prevent an increase in excessively recessed portions, and thus the formation of voids. The shape factor SF-2 is calculated from the following expression, i.e., by dividing the square of the projected perimeter L by the projected area S of a particle and 4π, followed by multiplication by 100:
- The shape factor SF-2 can be measured as in the measurement of the average plate diameter. An SEM image of ferrite particles is photographed with an FE-SEM, and the perimeter and projected area of each particle is measured using the automatic particle analyzing function of an EDX to calculate the shape factor SF-2 of the particle. Among the measured particles excluding those observed in the thickness direction, those fixed in a standing state during the FE-SEM observation, and those including a plurality of particles recognized as one particle, the average of 100 particles is defined as a shape factor SF-2.
- The platy ferrite particles preferably comprise Ni-Zn ferrite or Ni-Zn-Cu ferrite. These ferrites readily cause abnormal crystal growth, and can facilitate the production of a powdered ferrite containing platy ferrite particles having protrusions. Ni-Zn ferrite and Ni-Zn-Cu ferrite more readily cause abnormal crystal growth through control of only the oxygen content, specifically, a reduction of the oxygen content during the sintering step and/or heat treatment steps in the production of ferrite particles. Thus, these ferrites can more readily and effectively form platy ferrite particles having protrusions, compared to Mn-Zn ferrite or Mn ferrite. Ni-Zn ferrite or Ni-Zn-Cu ferrite can have any composition. In a preferred composition, the contents of Fe, Ni, Zn, and Cu elements are 45 to 52 wt%, 5 to 25 wt%, 0.5 to 25 wt%, and 0 to 6 wt%, respectively.
- The resin composition (resin molded article) according to the present invention is prepared through curing or thermosetting of a composition comprising a mixture of the powdered ferrite and a resin. The resin composition desirably contains 50 to 99.5 wt% powdered ferrite. At a content of 50 wt% or more, the composition can sufficiently demonstrate the characteristics of the ferrite. In contrast, a content of 99.5 wt% or less can facilitate the molding of the resin composition. The resin used in the resin composition preferably has flexibility. Such a flexible resin enables the resin composition to be processed to have a curved surface. Examples of the resin include, but should not be limited to, epoxy resins, phenol resins, melamine resins, urea resins, fluororesins, and poly(vinyl alcohol). This resin composition may contain a variety of additives, such as a curing agent, a curing accelerator, and silica particles, when necessary.
Fig. 1 illustrates an example cross-section of the resin composition. Aresin composition 1a illustrated inFig. 1 comprisespowdered ferrite 2a andresin 3. As described above, thecomposition 1a of flexible resin can be processed to have a curved surface. - The resin composition comprising the powdered ferrite as a filler can be used as an electromagnetic shielding material. This electromagnetic shielding material can be bonded to base bodies, and has high electromagnetic shielding characteristics derived from the powdered ferrite. In addition, the electromagnetic shielding material can have high flexibility attributed to high dispersibility of the powdered ferrite. Such high flexibility allows a high degree of freedom in shape of the body to be bonded to, and therefore, the electromagnetic shielding material can be bonded to a base body having a curved surface. The electromagnetic shielding material can be bonded to the base body by any means, for example, hydraulic transfer.
- The electronic circuit board, electronic circuit component, and housing for electronic devices according to the present invention comprise the electromagnetic shielding material, and have a high electromagnetic shielding effect. Due to high flexibility of the electromagnetic shielding material, the electronic circuit board, electronic circuit component, and housing for electronic devices according to the present invention have a high degree of freedom in shape, and can have curved surfaces to be bonded to the electromagnetic shielding material.
Fig. 2 is a sectional view illustrating an example housing for electronic devices which accommodates an electronic circuit. InFig. 2 , theresin composition 1a is disposed on and along the curved outer peripheral surface of anelectromagnetic wave shield 8 made of a metal, and serves as an electromagnetic shielding material. - The production of the powdered ferrite according to the present invention will now be described.
- For the production of the powdered ferrite according to the present invention, ferrite raw materials are weighed, and are mixed with a Henschel mixer or the like. Examples of the ferrite raw materials include, but should not be limited to, metal oxides, metal carbonates, metal hydroxides, and mixtures thereof. The mixture of ferrite raw materials can be pelletized with a roll compactor or the like, and is calcined in a rotary kiln or the like. The calcination is performed at a temperature of 1000°C in ambient atmosphere, for example.
- In the next step, the calcined product is coarsely and then finely milled. The water content is adjusted to yield cakes of calcined product. A dispersant is added to the cakes of calcined product, and is dispersed with a disperser to prepare aqueous ink. A binder is further added thereto to prepare ink for coating.
- The ink for coating is then applied into a predetermined thickness onto a base material, such as a film, using an applicator, for example. After the application of the ink, a PVA aqueous solution is further applied onto the ink coated surface, and water is removed. The ink coated surface is peeled off from the base material to yield a platy granulated product (ferrite precursor) before sintering.
- The binder is removed from the platy granulated product (ferrite precursor) before sintering, followed by sintering the platy granulated product. The binder removal is preferably performed at a temperature equal to or lower than the sintering temperature preferably under a condition such that the binder component can be removed. The sintering can be performed at a temperature of about 800 to 1300°C in an atmosphere where the oxygen content is 20 vol% or less, preferably 3.5 vol% or less. Such a reduced oxygen content can form protrusions accompanied by the abnormal crystal growth. On the other hand, in the case where a heat treatment is performed as described later, the sintering may be performed in ambient atmosphere.
- The ferrite precursor before the sintering and/or the sintered product after the sintering may be milled to adjust the plate diameter, when necessary. Platy ferrite particles having a predetermined shape can be readily produced through the milling. In the milling, the ferrite precursor before the sintering and/or the sintered product after the sintering may be milled, and may be classified through a sieve having a predetermined opening to have a target plate diameter. The adjustment of the plate diameter through the milling may be performed after the sintering, or may be performed before the binder removal and/or sintering steps to prevent the fusion between the particles during the sintering step. In this specification, the milling performed before the sintering is referred to as pre-sintering milling, and the milling performed after the sintering is referred to as post-sintering milling for clarity, when necessary.
- In the case where the milling is performed after the sintering (post-sintering milling), a heat treatment (annealing) may be performed after the milling as necessary. The direction of crystal growth of the platy ferrite particles is substantially restricted to the plane direction thereof, and therefore, the platy ferrite particles have a crystal structure which is more readily distorted than bulky ferrite. Furthermore, the crystal structure of the ferrite particles is more likely to be distorted through the milling. The distortion of the crystal structure can be reduced through the heat treatment performed after the sintering and milling steps. The heat treatment may be performed at a temperature of about 800 to 1300°C in an atmosphere where the oxygen content is 20 vol% or less, preferably 3.5 vol% or less. Such a reduced oxygen content can form protrusions accompanied by the abnormal crystal growth.
- The powdered ferrite prepared through these steps comprises platy ferrite particles having protrusions having a specific shape on the surfaces thereof. Such a powdered ferrite has high dispersibility in resins and a significantly increased plate diameter, thus achieving high electromagnetic shielding characteristics. In addition, the powdered ferrite also has high productivity. The resin compositions and the electromagnetic shielding materials comprising the powdered ferrite as a filler have high flexibility attributed to high dispersibility of the powdered ferrite, and can be bonded to base bodies (housings) having curved surfaces.
- In contrast, the methods disclosed in Citation List have difficulties in production of platy powdered ferrite having high dispersibility and productivity together with a large plate diameter. For example, in the methods disclosed in Patent Literatures 1 to 3, the length
- (long diameter) in the plane direction is inevitably restricted. In addition, the thickness may be increased depending on the method of producing a sheet, substantially precluding powdered ferrite having a desired aspect ratio. Patent Literature 2 does not disclose any information on the shape of the particles of the powdered ferrite other than the long diameter, the plate thickness, and the aspect ratio thereof.
Patent Literature 3 discloses ferrite particles having indefinite shapes and a platy shape. However, in the method disclosed in this literature, a sufficient aspect ratio cannot be achieved due to a significantly small ferrite particle diameter, or the grain size of the ferrite particles cannot be sufficiently ensured due to a significantly low sintering temperature. As a result, the powdered ferrite may inevitably have a low magnetic permeability, which is used as a substituting index indicating the electromagnetic wave absorbing characteristics. - In the case where the ferrite sheet is prepared by peeling off from the film to obtain the ferrite sheet solely as disclosed in Patent Literature 4, the ferrite sheet could be broken. It is difficult to obtain the powdered ferrite in a stable state. In particular, a thinner ferrite sheet is more difficult to peel off from the base material, imposing more difficulties in the actual production process. To avoid the breakage of the ferrite sheet during the peeling-off stage from the film, a large amount of binder components needs to be added to a mixed coating solution. An increase in binder components will increase the viscosity of the coating solution containing the ferrite raw material. The content of the ferrite raw material in the coating solution could be reduced to adjust the viscosity. However, in such a case, holes are readily formed during the sintering of the ferrite sheet. The holes formed may cause a reduction in magnetic permeability, which is used as a substituting index indicating the electromagnetic shielding characteristics. The method disclosed in Patent Literature 5, on the other hand, offers a clue to solve the problems in the related art. Unfortunately, since ager is used as the binder, the ink (slurry) should be always kept at a specific temperature during the application of the ink, which imposes difficulties in productivity.
- The present invention will now be described in more detail by way of Examples.
- A powdered ferrite was prepared in accordance with the following procedure. Detailed conditions for production are also shown in Table 1.
- Iron oxide, nickel oxide, zinc oxide, and copper oxide as raw materials were weighed such that the amounts of Fe2O3, NiO, ZnO, and CuO were 51.5 mol, 15 mol, 30 mol, and 8 mol, respectively, and were mixed with a Henschel mixer. The mixture was pelletized with a roll compactor, and was calcined with a rotary kiln in ambient atmosphere at a temperature of 950°C. A calcined product was thereby yielded.
- Ink was prepared from the calcined product. The calcined product was coarsely milled with a rod mill, and then finely milled with a wet bead mill. The water content was adjusted to give a solid content of 65 wt%. Cakes of the calcined product were thereby yielded. A dispersant was added to the cakes of the calcined product, and was dispersed with a homogenizer to prepare aqueous ink. A poly(vinyl alcohol) (PVA) binder was further added to the aqueous ink in an amount of 5 wt% of the water content in the aqueous ink. Ink for coating was thereby prepared.
- A ferrite precursor was prepared with the resulting ink for coating. The ink was applied onto a base material. The ink was applied onto a commercially available PET film (thickness: 50 µm), i.e. base material, with an applicator into a film having a thickness after drying (dry thickness) of 10 µm. After the coating of the ink, water was removed from the coated surface. A PVA aqueous solution (25 wt% aqueous solution) was further applied onto the ink coated surface, and was dried. The coated surface was peeled off from the base material to prepare a green platy granulated product (ferrite precursor) in the form of a sheet.
- The binder was removed from the ferrite precursor in the air at 650°C. The ferrite precursor was then sintered at 1200°C for four hours in an atmosphere containing 0 vol% oxygen, yielding a platy sintered product.
- The platy sintered product was milled (post-sintering milling) to yield a powdered ferrite. The sintered and milled product was classified with sieves (36 mesh and 80 mesh) in accordance with Japanese Industrial Standards (JIS). The powdered ferrite contained platy ferrite particles having an average thickness of 8 µm and an average plate diameter of 489 µm.
- A powdered ferrite was prepared as in Example 1 except that the dry thickness during the application of the ink was 3.5 µm, the binder was removed at a temperature of 1000°C, and sieves (80 mesh and 250 mesh) in accordance with JIS were used in the milling.
- A powdered ferrite was prepared as in Example 2 except that the sintering was performed in ambient atmosphere, and a heat treatment was performed at 1220°C in an atmosphere containing 0 vol% oxygen after the milling.
- A powdered ferrite was prepared as in Example 1 except that raw materials, i.e., iron oxide (Fe2O3), nickel oxide (NiO), zinc oxide (ZnO), and copper oxide (CuO) were compounded in amounts of 49 mol, 15 mol, 30 mol, and 6 mol, respectively, the dry thickness after the application of the ink was 9 µm, and sieves (80 mesh and 250 mesh) in accordance with JIS were used in the milling.
- A powdered ferrite was prepared as in Example 1 except that raw materials, i.e., iron oxide (Fe2O3), nickel oxide (NiO), zinc oxide (ZnO), and copper oxide (CuO) were compounded in amounts of 52.75 mol, 15 mol, 30 mol, and 9 mol, respectively, the dry thickness during the application of the ink was 11 µm, and sieves in accordance with JIS (250 mesh and 350 mesh) were used in the milling.
- A powdered ferrite was prepared as in Example 2 except that the milling before sintering (pre-sintering milling) was performed rather than the milling after the sintering (post-sintering milling). In the pre-sintering milling, a ferrite precursor after the binder removal was milled, and was classified with sieves (36 mesh and 80 mesh) in accordance with JIS.
- A powdered ferrite was prepared as in Example 2 except that the sintering temperature was 1090°C, and sieves (36 mesh and 80 mesh) in accordance with JIS were used in the milling.
- A powdered ferrite was prepared as in Example 7 except that the sintering temperature was 1250°C.
- A powdered ferrite was prepared as in Example 2 except that the sintering was performed in an atmosphere containing 8 vol% oxygen, and the milling (post-sintering milling) was not performed.
- A powdered ferrite was prepared as in Example 1 except that the binder was removed at a temperature of 1000°C and the sintering was performed in ambient atmosphere.
- A powdered ferrite was prepared as in Example 10 except that a heat treatment was performed at 1220°C in ambient atmosphere after the milling (post-sintering milling) was performed.
- A powdered ferrite was prepared as in Example 2 except that the PVA aqueous solution was not applied during the preparation of the ferrite precursor, the sintering was performed in ambient atmosphere, and a sieve (350 mesh) in accordance with JIS was used in the milling (post-sintering milling).
- A powdered ferrite was prepared as in Example 1 except that the binder was removed at a temperature of 1000°C and the sintering temperature was 1050°C.
- A powdered ferrite was prepared as in Example 13 except that the sintering temperature was 1310°C.
- Characteristics of the powdered ferrite in Examples 1 to 14 were evaluated as follows.
- The composition of the powdered ferrite was determined by chemical analysis. Ferrite particles (0.2 g) were weighed, and were completely dissolved in a heated solution of 1N hydrochloric acid (20 ml) and 1N nitric acid (20 ml) in pure water (60 ml) to prepare an aqueous solution. The contents of the metal elements in the aqueous solution were determined with an ICP analyzer (SHIMADZU Corporation, ICPS-1000IV). Similarly, the contents of the metal elements in Examples and Comparative Examples described later were also determined.
- The average plate diameter and the shape factor SF-2 were determined at the same time . An SEM image of ferrite particles was photographed with an FE-SEM. The length, perimeter, and projected area of each particle were measured using the automatic particle analyzing function of an EDX to calculate the length of each particle. Among the measured particles excluding those observed in the thickness direction, those fixed in a standing state during the FE-SEM observation, and those including a plurality of particles recognized as one particle, the lengths of 100 particles were averaged to determine the average plate diameter. The SF-2 was determined from the perimeter and projected area of each particle, and the average of 100 particles was defined as a shape factor SF-2. The SEM image was photographed with an FE-SEM SU-8020 made by Hitachi High-Technologies Corporation at an accelerating voltage of 15 KV and a magnification of 200x, and was subjected to particle analysis with an EDX X-MAX made by HORIBA, Ltd. while image information was being received from the FE-SEM.
- The average thickness of the platy ferrite particles was determined as follows. Powdered ferrite (9 g) and powder resin (1 g) were placed into a 50-cc glass bottle, and were mixed in a ball mill for 30 minutes. The mixture was placed into a die having a diameter of 13 mm, and was molded under a pressure of 30 MPa. The molded article in a vertically standing state was then embedded in a resin such that the cross-section of the molded article was observed. The molded article was polished with an abrasive machine, and was used as a sample for measuring the thickness of the ferrite particle. The sample for measuring the thickness of the ferrite particle was photographed at a magnification of 50x to 800x with an SEM, and the thickness (length in the minor axis direction) of each particle was measured in disregard of protrusions from the particle in the SEM image. The arithmetic average of the thicknesses of 100 particles was calculated, and was defined as the average thickness of the ferrite particles.
- The aspect ratio of the platy ferrite particles was calculated as an aspect ratio (average plate diameter)/(average thickness) from the average plate diameter and the average thickness described above.
- The heights of protrusions of the platy ferrite particles were determined as follows: A cross-section of a sample was prepared as in the determination of the average thickness of the platy ferrite particles, and the heights of the protrusions from the surfaces of the particle were measured. An SEM image was photographed as described above. In the case where the number of protrusions is small, it is difficult to observe a sufficient number of samples in the cross-sectional area. In such a case, an SEM image of particles was photographed as in the determination of the average plate diameter, and was printed out. The particles substantially standing upright were selected from the photographed image, and the thicknesses of the platy particles and the heights of the protrusions were directly measured with a scale. In either case, 100 particles having protrusions were selected, and the heights of the protrusions of the particles were measured. The arithmetic average was defined as the height of the protrusions.
- The proportion of platy ferrite particles (particles with protrusions) each having at least one protrusion on the surface thereof contained in the powdered ferrite was determined as follows: An SEM image was photographed as in the measurement of the height of protrusions. The total number of particles and the number of particles with protrusions in the SEM image were visually counted. The proportion of the particles with protrusions was calculated from (the number of particles with protrusions)/(the total number of particles).
- The magnetic characteristics of the powdered ferrite were measured with a vibrating sample magnetometer (Toei Industry Co., Ltd., VSM-C7-10A). A sample (powdered ferrite) was filled in a cell having an inner diameter of 5 mm and a height of 2 mm. The cell was placed in the magnetometer. During the measurement, a magnetic field was applied, and was swept up to 5 K·1000/4π·A/m. In the next step, the applied magnetic field was decreased to print a hysteresis curve on a recording paper. From the data in this curve, the magnetization (σs) was read at an applied magnetic field of 5 K·1000/4π·A/m. The residual magnetization (σr) and the coercive force (Hc) were also obtained.
- The frequency characteristics of the powdered ferrite were determined through the measurement of the complex magnetic permeability of the powdered ferrite. For the measurement of the complex magnetic permeability, a sample was prepared as follows. Powdered ferrite (9 g) and binder resin (Kynar301F: poly(vinylidene fluoride)) (1 g) were weighed, were placed into a 50-cc glass bottle, and were mixed under stirring with a ball mill at 100 rpm for 30 minutes. After stirring, about 0.6 g of the mixture was weighed, and was placed into a die having an inner diameter of 4.5 mm and an outer diameter of 13 mm. The mixture was pressed with a press under a pressure of 40 MPa for one minute. The molded article was settled in a hot air dryer at 140°C for two hours to prepare a sample for measuring the complex magnetic permeability. The complex magnetic permeability was measured with an RF impedance/material analyzer (Agilent Technologies, Inc., E4991A) and a measuring electrode for a magnetic material (Agilent Technologies, Inc., 16454A). The outer diameter, the length in the minor axis direction, and the inner diameter of the sample were measured, and were input into the analyzer. The complex magnetic permeability (real part µ' and imaginary part µ" of the magnetic permeability) was measured at an amplitude of 100 mV where sweeping was performed in the range of 1 MHz to 1 GHz in logarithmic terms. Table 2 shows the magnetic permeabilities µ' and µ" at 13.56 MHz.
- The flexibility of the resin molded article comprising the powdered ferrite was evaluated. For the evaluation, the resin molded article was prepared as follows: A binder resin (10 wt% PVA aqueous solution) (45 g) and powdered ferrite (5 g) were mixed to disperse the powdered ferrite. The dispersion was suction-filtered through a Nutsche funnel having a diameter of 180 mm to deposit a layer of platy ferrite particles containing the binder resin on a filter paper. The layer of the platy ferrite particles was dried to remove water. The layer was then peeled off from the filter paper, and was cut into a 30 mm square to prepare a sheet containing the platy ferrite particles. The sheet was used as a resin molded article. The resin molded article was then bent along an acrylic round bar having a diameter of 20 mm to evaluate the flexibility. The flexibility was ranked according to the following criteria:
- Rank A: The resin molded article was rounded without breaking.
- Rank B: The resin molded article was rounded with cracks.
- Rank C: The resin molded article was broken.
- The powdered ferrites in Examples 1 to 9 had not only superior magnetic characteristics and frequency characteristics but also high flexibility in the form of the resin molded articles. In contrast, the powdered ferrites in Examples 10 to 13 (Comparative) had poor flexibility in the form of the resin molded articles, i.e., were cracked or broken. In Example 14, powdered ferrite was not yielded because of the fusion between the particles during the sintering step.
- An SEM image of the powdered ferrite in Example 1 is shown in
Fig. 3. Fig. 3 demonstrates that individual platy ferrite particles have indefinite shapes, and each have at least one protrusion on its surface, the at least one protrusion having a shape selected from the group consisting of a rectangular pyramid, a truncated rectangular pyramid, an elongated rectangular pyramid, and combinations thereof. - Furthermore, the resin molded article prepared in Example 2 was put on water, and was bonded onto the surface of a plastic base body through hydraulic transfer to prepare a housing. Although the housing had a curved surface, the ferrite particles were successfully bonded to the housing along the curved surface. It was confirmed that the ferrite particles are applicable to curved surfaces without difficulty.
-
Table 1 Amounts Calcining Preparation of ink Preparation of ferrite precursor Binder removal Pre-sintering milling Sintering Post-sintering milling Heat treatment Fe2O3 (mol) NiO (mol) ZnO (mol) CuO (mol) Temp. (°C) Atmosphere Particle diameter in Slurry (µm) Ink Viscosity (cps) Ink Coating thickness (dry thickness, µm) PVA Coating thickness (wet thickness, µm) Temp. (°C) Atmosphere Milliing condition (mesh) Temp. (°C) Atmosphere (O2 content) Milling condition (mesh) Temp. (°C) Atmosphere (O2 content) Ex. 1 51.5 15 30 8 950 Ambient 0.85 800 10 120 650 Ambient - 1200 0 vol% 36/80 - - Ex. 2 51.5 15 30 8 950 Ambient 0.85 800 3.5 250 1000 Ambient - 1200 0 vol% 80/250 - - Ex. 3 51.5 15 30 8 950 Ambient 0.85 800 3.5 250 1000 Ambient - 1200 Ambient 80/250 1220 0 vol% Ex. 4 49 15 30 6 950 Ambient 0.91 650 9 120 650 Ambient - 1200 0 vol% 80/250 - - Ex. 5 52.75 15 30 9 950 Ambient 0.80 900 11 120 650 Ambient - 1200 0 vol% 250/350 - - Ex. 6 51.5 15 30 8 950 Ambient 0.85 800 3.5 250 1000 Ambient 36/80 1200 0 vol% - - - Ex. 7 51.5 15 30 8 950 Ambient 0.85 800 3.5 250 1000 Ambient - 1090 0 vol% 36/80 - - Ex. 8 51.5 15 30 8 950 Ambient 0.85 800 3.5 250 1000 Ambient - 1250 0 vol% 36/80 - - Ex. 9 51.5 15 30 8 950 Ambient 0.85 800 3.5 250 1000 Ambient - 1200 8 vol% - - - Ex. 10* 51.5 15 30 8 950 Ambient 0.85 800 10 120 1000 Ambient - 1200 Ambient 36/80 - - Ex. 11* 51.5 15 30 8 950 Ambient 0.85 800 10 120 1000 Ambient - 1200 Ambient 36/80 1220 Ambient Ex. 12* 51.5 15 30 8 950 Ambient 0.85 800 3.5 - 1000 Ambient - 1200 Ambient -350 - - Ex. 13* 51.5 15 30 8 950 Ambient 0.85 800 10 120 1000 Ambient - 1050 0vol% 36/80 - - Ex. 14* 51.5 15 30 8 950 Ambient 0.85 800 10 120 1000 Ambient - 1310 0vol% 36/80 - - indicates Comparative Example. Temp. = Temperature -
Table 2 Chemical analysis (wt%) Characteristics of powder Magnetic characteristics Frequency characteristics Flexibility of resin molded article Fe Ni Zn Cu Proportion of particles with protrusions (number %) Height of protrusion (µm) Average plate diameter (µm) Average thickness (µm) Aspect ratio SF-2 σs (emu/g) σr (emu/g) Hc (Oe) µ' µ" Ex. 1 46.26 6.82 16.15 4.05 100 2 489 8 61.13 262 63.24 2.239 22.18 29 3 A Ex. 2 46.77 7.05 15.81 4.08 95 2 314 2.5 125.60 169 63.24 2.239 22.18 32 3 A Ex. 3 46.75 7.02 16.09 3.96 97 2.5 314 2.5 125.60 169 63.24 2.239 22.18 35 3 A Ex. 4 45.85 7.38 16.20 3.68 89 2 235 8 29.38 158 61.79 2.58 23.5 31 4 A Ex. 5 46.19 6.54 15.31 4.00 84 2 82 8 10.25 144 63.36 2.12 22.28 25 2 A Ex. 6 45.98 6.76 16.20 4.57 87 2 314 2.5 125.60 149 63.24 2.239 22.18 34 3 A Ex. 7 46.69 7.07 15.73 3.72 65 1 152 2.5 60.80 150 63.24 2.239 22.18 26 2 A Ex. 8 46.42 7.21 15.60 3.63 100 2.5 53 2.5 21.20 146 63.24 2.239 22.18 32 2 A Ex. 9 46.42 7.21 15.60 3.63 52 1.5 53 2.5 21.20 156 63.24 2.239 22.18 27 2 A Ex. 10* 46.17 6.98 15.33 4.45 0 0 27 8 3.38 119 63.24 2.239 22.18 23 2 B Ex. 11* 46.17 6.98 15.33 4.45 0 0 27 12 2.25 123 63.24 2.239 22.18 23 2 C Ex. 12* 46.45 7.20 15.79 4.42 0 0 24.2 2.5 9.68 127 63.24 2.239 22.18 8 1 B Ex. 13* 46.17 6.98 15.33 4.45 28 1 27 8 3.38 124 63.24 2.239 22.18 19 4 B Ex. 14* - - - - - - - - - - - - - - - - * indicates Comparative Example.
Claims (12)
- A powdered ferrite comprising platy ferrite particles having a spinel crystal structure,
wherein the powdered ferrite comprises at least 50 number % platy ferrite particles each having at least one protrusion on a surface of the particle, and the at least one protrusion has a shape selected from the group consisting of a rectangular pyramid, a truncated rectangular pyramid, an elongated rectangular pyramid, and combinations thereof. - The powdered ferrite according to claim 1, wherein the height of the protrusion is smaller than the thickness of the platy ferrite particle.
- The powdered ferrite according to claim 1 or 2, wherein the platy ferrite particles have an average plate diameter of 10 to 2000 µm.
- The powdered ferrite according to any one of claims 1 to 3, wherein the platy ferrite particles have an average thickness of 0.5 to 100 µm.
- The powdered ferrite according to any one of claims 1 to 4, wherein the platy ferrite particles have an aspect ratio of 4 to 1000.
- The powdered ferrite according to any one of claims 1 to 5, wherein the platy ferrite particles have indefinite shapes.
- The powdered ferrite according to claim 6, wherein the platy ferrite particles have a shape factor SF-2 of 135 to 300.
- The powdered ferrite according to any one of claims 1 to 7, wherein the platy ferrite particles comprise Ni-Zn ferrite or Ni-Zn-Cu ferrite.
- A resin composition, comprising the powdered ferrite according to any one of claims 1 to 8 and a resin.
- An electromagnetic shielding material, comprising the powdered ferrite according to any one of claims 1 to 8 as a filler.
- The electromagnetic shielding material according to claim 10, wherein the electromagnetic shielding material has flexibility, and is bondable to a base body having a curved surface.
- An electronic circuit board, electronic circuit component, or housing for electronic devices, comprising the powdered ferrite according to any one of claims 1 to 8 and/or the resin composition according to claim 9 and/or the electromagnetic shielding material according to claims 10 and 11, wherein the electronic circuit board, electronic circuit component, or housing for electronic devices has an electromagnetic shielding effect.
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PCT/JP2017/014263 WO2017191725A1 (en) | 2016-05-02 | 2017-04-05 | Ferrite powder, resin composition, electromagnetic shielding material, electronic circuit substrate, electronic circuit component, and electronic device housing |
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